Molecular Biology and Evolution, Vol 9, 235-249, Copyright © 1992 by Society for Molecular Biology and Evolution
JM Turbeville, KG Field and RA Raff
Partial 18S rRNA sequence of the nemertine Cerebratulus lacteus was
obtained and compared with those of coelomate metazoans and acoelomate
platyhelminths to test whether nemertines share a most recent common
ancestor with the platyhelminths, as traditionally has been implied, or
whether nemertines lie within a protostome coelomate clade, as suggested by
more recent morphological analyses. Maximum-parsimony analysis supports the
inclusion of the nemertine within a protostome- coelomate clade that falls
within a more inclusive coelomate clade. Bootstrap analysis indicates
strong support for a monophyletic Coelomata composed of a deuterostome and
protostome-coelomate clade. Support for a monophyletic protostome Coelomata
is weak. Inference by distance analysis is consistent with that of maximum
parsimony. Analysis of down-weighted paired sites by maximum parsimony
reveals variation in topology only within the protostome-coelomate clade.
The relationships among the protostome coelomates cannot be reliably
inferred from the partial sequences, suggesting that coelomate protostomes
diversified rapidly. Results with evolutionary parsimony are consistent
with the inclusion of the nemertine in a coelomate clade. The molecular
inference corroborates recent morphological character analyses that reveal
no synapomorphies of nemertines and flatworms but instead suggest that the
circulatory system and rhynchocoel of nemertines are homologous to coelomic
cavities of protostome coelomates, thus supporting the corresponding
hypothesis that nemertines belong within a protostome-coelomate clade. The
sequence data provide an independent test of morphological character
homology.
ORIGINAL ARTICLE
Phylogenetic position of phylum Nemertini, inferred from 18S rRNA sequences: molecular data as a test of morphological character homology
Department of Biology, Indiana University, Bloomington 47405.
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